Skip to main content

dg health omeprazole

NDC 55910-712 · Dolgencorp Inc

Generic nameomeprazole
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE
Strength20 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryNDA

Packages

55910-712-01 — 1 BOTTLE in 1 CARTON (55910-712-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

55910-712-03 — 3 BOTTLE in 1 CARTON (55910-712-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55111-157 — Omeprazole, 55111-158 — Omeprazole, 55111-159 — Omeprazole, 55111-643 — Omeprazole, 55111-644 — Omeprazole, 55111-645 — Omeprazole, 55154-2332 — Omeprazole, 55301-915 — Omeprazole, 55681-306 — OMEPRAZOLE, 55910-215 — Omeprazole, 55910-713 — omeprazole, 55910-915 — Omeprazole, 56062-401 — Omeprazole, 56062-915 — Omeprazole, 57237-160 — Omeprazole, 57237-161 — Omeprazole, 57237-162 — Omeprazole, 57483-840 — omeprazole, 57896-659 — Omeprazole, 58602-725 — OMEPRAZOLE AND SODIUM BICARBONATE, +295 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.